3-Hydroxy-2-nitropyridine - ≥98% , CAS No.15128-82-2

CAS: 15128-82-2 Cat. No.: H119963 Formule: C5H4N2O3 Poids moléculaire: 140.1 Beilstein Registry Number: 124473 Numéro CE: 239-191-2
DISPONIBLE À COMMANDE
GRADE & PURITY ≥98%
Synonyms
2-Nitro-pyridin-3-ol | 2-Nitropyridin-3-ol | FT-0615808 | AKOS000120717 | BP-11548 | UNII-UU357X85YB | W-108063 | 2-Nitro-3-hydroxypyridine | 2-Nitro3-hydroxy-pyridine | 2-Nitro-3-pyridinol | 3-PYRIDINOL, 2-NITRO- | J-200148 | SY002996 | Q27291274 | NSC 9
Storage
Room temperature
Shipped In
Normal
★
Size
USA
Allemagne (EU)*
Price
Qty
5g
H119963-5g
Sur commande · 8–12 semaines
9,90$US
10g
H119963-10g
1 En stock
—
10,90$US
25g
H119963-25g
1 En stock
—

16,90$US

25,90$US
Enregistrer 9,00 $US (34.75%)
50g
H119963-50g
5 En stock
—

30,90$US

46,90$US
Enregistrer 16,00 $US (34.12%)
100g
H119963-100g
3 En stock
—

52,90$US

79,90$US
Enregistrer 27,00 $US (33.79%)
250g
H119963-250g
Sur commande · 8–12 semaines

115,90$US

173,90$US
Enregistrer 58,00 $US (33.35%)
500g
H119963-500g
Sur commande · 8–12 semaines

160,90$US

241,90$US
Enregistrer 81,00 $US (33.48%)
Enter a quantity for the sizes you want to add.
🧪

Why this grade

≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Room temperature Ships Normal Check lot-specific COA for exact specifications.

📋

Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Synonymes
2-Nitro-pyridin-3-ol | 2-Nitropyridin-3-ol | FT-0615808 | AKOS000120717 | BP-11548 | UNII-UU357X85YB | W-108063 | 2-Nitro-3-hydroxypyridine | 2-Nitro3-hydroxy-pyridine | 2-Nitro-3-pyridinol | 3-PYRIDINOL, 2-NITRO- | J-200148 | SY002996 | Q27291274 | NSC 9
Spécifications et pureté
≥98%
Conditions de stockage de stockage
Room temperature
Expédié en
Normal
Pureté
≥98%
Noms et identifiants
Pubchem Sid488183038
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488183038
Sourires canoniquesC1=CC(=C(N=C1)[N+](=O)[O-])O
IUPAC Name2-nitropyridin-3-ol
InChIKeyQBPDSKPWYWIHGA-UHFFFAOYSA-N
INCHI1S/C5H4N2O3/c8-4-2-1-3-6-5(4)7(9)10/h1-3,8H
Isomères SMILES C1=CC(=C(N=C1)[N+](=O)[O-])O
WGK Allemagne 3
RTECS UU7715000
Poids moléculaire 140.1
Beilstein 124473
Reaxy-Rn 124473
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=124473&ln=

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganic 1,3-dipolar compounds
ClasseAllyl-type 1,3-dipolar organic compounds
SubclassOrganic nitro compounds
Intermediate Tree Nodes C-nitro compounds
Direct ParentNitroaromatic compounds
Alternative Parents Hydroxypyridines  Imidolactams  Heteroaromatic compounds  Propargyl-type 1,3-dipolar organic compounds  Organic oxoazanium compounds  Azacyclic compounds  Organopnictogen compounds  Organooxygen compounds  Organonitrogen compounds  Organic zwitterions  Organic oxides  Hydrocarbon derivatives  
Molecular FrameworkAromatic heteromonocyclic compounds
Substituents Nitroaromatic compound - Hydroxypyridine - Pyridine - Imidolactam - Heteroaromatic compound - Organic oxoazanium - Propargyl-type 1,3-dipolar organic compound - Organoheterocyclic compound - Azacycle - Organonitrogen compound - Organic oxygen compound - Organic zwitterion - Organic nitrogen compound - Organooxygen compound - Organopnictogen compound - Hydrocarbon derivative - Organic oxide - Aromatic heteromonocyclic compound
DescriptionThis compound belongs to the class of organic compounds known as nitroaromatic compounds. These are c-nitro compounds where the nitro group is C-substituted with an aromatic group.
External Descriptors Not available
Structure 3D
Modèle de structure chimique interactif





Certificats (CoA, COO, BSE/TSE et tableau d'analyse)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

9 results found

Lot NumberCertificate TypeDateArticle
J2219161Certificate of AnalysisJul 30, 2026 H119963
H2124009Certificate of AnalysisJun 11, 2025 H119963
H2124010Certificate of AnalysisJun 11, 2025 H119963
J2421585Certificate of AnalysisJun 14, 2024 H119963
J2421586Certificate of AnalysisJun 14, 2024 H119963
K1828142Certificate of AnalysisSep 19, 2022 H119963
G2215639Certificate of AnalysisJun 08, 2022 H119963
G2215641Certificate of AnalysisJun 08, 2022 H119963
G2215642Certificate of AnalysisJun 08, 2022 H119963
Propriétés chimiques et physiques
SensibilitéAir Sensitive
Point de fusion (°C)71°C
Poids moléculaire140.100 g/mol
XLogP31.200
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count4
Rotatable Bond Count0
Exact Mass140.022 Da
Monoisotopic Mass140.022 Da
Topological Polar Surface Area78.900 Ų
Heavy Atom Count10
Formal Charge0
Complexity133.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Calculateurs de solution
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